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filingDate 2004-02-06^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-05-31^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_083cbf977d7a39c313723e3afc8a22a9
publicationDate 2005-05-31^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6900211-B2
titleOfInvention CCR5 antagonists useful for treating aids
abstract Compounds of the formula n n nor a pharmaceutically acceptable salt or isomer thereof, wherein:n Q, X and Z are CH or N; R, R 4 -R 7 and R 13 are H or alkyl; R 1 is H, alkyl, fluoroalkyl, R 9 -arylalkyl, R 9 -heteroarylalkyl, alkyl-SO 2 —, cycloalkyl-SO 2 —, fluoroalkyl-SO 2 —, R 9 -aryl-SO 2 —, R 9 -heteroaryl-SO 2 —, N(R 22 )(R 23 )—SO 2 —, alkyl-C(O)—, cycloalkyl-C(O)—, fluoroalkyl-C(O)—, R 9 -aryl-C(O)—, NH-alkyl-C(O)— or R 9 -aryl-NH—C(O)—; R 2 is H and R 3 is H, alkyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, R 9 -aryl, R 9 -arylalkyl, R 9 -heteroaryl, or R 9 -heteroarylalkyl, and when X and Z are each CH, R 3 is alkoxy, R 9 -aryloxy, R 9 -heteroaryloxy, alkylC(O)O—, alkylaminoC(O)O—, alkylC(O)NR 13 —, alkylOC(O)NR 13 — or alkylaminoC(O)NR 13 —; or R 2 and R 3 together are ═O, ═NOR 10 , ═N—NR 11 R 12 or ═CH-alkyl; R 8 is substituted phenyl, substituted heteroaryl, naphthyl, fluorenyl, diphenymethyl, alpha-substituted benzyl or alpha-substituted heteroarylmethyl; R 9 -R 12 are as defined;n nare disclosed for the treatment of HIV, solid organ transplant rejection, graft v. host disease, inflammatory diseases, atopic dermatitis, asthma, allergies or multiple sclerosis, as well as pharmaceutical compositions and combinations with antiviral or anti-inflammatory agents.
priorityDate 2001-03-29^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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